Nxthera, Inc. is one of 17539 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Nxthera, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Rezum System, Rezum System, Rezum System
3
Total
3
Cleared
0
Denied
Nxthera, Inc. has 3 FDA 510(k) cleared medical devices. Based in Maple Grove, US.
Historical record: 3 cleared submissions from 2015 to 2018. Primary specialty: Gastroenterology & Urology.
Browse the FDA 510(k) cleared devices submitted by Nxthera, Inc. Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Libramedical, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Nxthera, Inc.
3 devices